Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2010 1
2011 1
2015 1
2016 2
2017 2
2018 1
2022 2
2023 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

8 results

Results by year

Filters applied: . Clear all
Page 1
[Respiratory physiotherapy in pediatric practice].
Audag N, Dubus JC, Combret Y. Audag N, et al. Rev Mal Respir. 2022 Jun;39(6):547-560. doi: 10.1016/j.rmr.2022.05.001. Epub 2022 Jun 21. Rev Mal Respir. 2022. PMID: 35738979 Review. French.
For LRT clearance, several indications, such as cystic fibrosis, primary ciliary dyskinesia and neuromuscular disease, are now widely advocated. ...
For LRT clearance, several indications, such as cystic fibrosis, primary ciliary dyskinesia and neuromuscular disease, …
Treatment recommendations in Primary Ciliary Dyskinesia.
Polineni D, Davis SD, Dell SD. Polineni D, et al. Paediatr Respir Rev. 2016 Mar;18:39-45. doi: 10.1016/j.prrv.2015.10.002. Epub 2015 Oct 20. Paediatr Respir Rev. 2016. PMID: 26586601 Review.
Primary Ciliary Dyskinesia (PCD) is a rare heterogenic disorder leading to significant respiratory morbidity. ...
Primary Ciliary Dyskinesia (PCD) is a rare heterogenic disorder leading to significant respiratory morbidity. ...
Underlying causes and outcomes of recurrent pneumonia in hospitalized children.
Mei M, Dai D, Guo Z, Zhang C, Liu J, Qi Y, Wang X, Wang L, Qian L. Mei M, et al. Pediatr Pulmonol. 2023 Jun;58(6):1674-1682. doi: 10.1002/ppul.26374. Epub 2023 Mar 21. Pediatr Pulmonol. 2023. PMID: 36919525 Review.
RESULTS: Of 551 children with RP, 483 (87.7%) manifested underlying causes, with recurrent aspiration (127, 23.0%), primary immunodeficiency (PID) (91, 16.5%), and congenital heart diseases (63, 11.4%) being the most common. ...PID odds ratio (OR, 7.9; 95% confidence inter …
RESULTS: Of 551 children with RP, 483 (87.7%) manifested underlying causes, with recurrent aspiration (127, 23.0%), primary immunodef …
Prevalence of primary ciliary dyskinesia in consecutive referrals of suspect cases and the transmission electron microscopy detection rate: a systematic review and meta-analysis.
Kouis P, Yiallouros PK, Middleton N, Evans JS, Kyriacou K, Papatheodorou SI. Kouis P, et al. Pediatr Res. 2017 Mar;81(3):398-405. doi: 10.1038/pr.2016.263. Epub 2016 Dec 9. Pediatr Res. 2017. PMID: 27935903 Review.
Diagnostic testing for primary ciliary dyskinesia (PCD) usually includes transmission electron microscopy (TEM), nasal nitric oxide, high-speed video microscopy, and genetics. ...Meta-analyses of pooled PCD prevalence and TEM detection rate across studies wer …
Diagnostic testing for primary ciliary dyskinesia (PCD) usually includes transmission electron microscopy (TEM), nasal …
[Pathogenic genes and corresponding ciliary defects associated with primary ciliary dyskinesia].
Wang L, Xu B, Gao L. Wang L, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022 Apr 10;39(4):433-437. doi: 10.3760/cma.j.cn511374-20201222-00898. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022. PMID: 35446983 Review. Chinese.
Primary ciliary dyskinesia (PCD) is a recessive genetic disorder of motile cilia with substantial genetic and phenotypic heterogeneity. ...
Primary ciliary dyskinesia (PCD) is a recessive genetic disorder of motile cilia with substantial genetic and phenotypi
Nasal polyposis pathophysiology: Endotype and phenotype open issues.
Brescia G, Zanotti C, Parrino D, Barion U, Marioni G. Brescia G, et al. Am J Otolaryngol. 2018 Jul-Aug;39(4):441-444. doi: 10.1016/j.amjoto.2018.03.020. Epub 2018 Mar 7. Am J Otolaryngol. 2018. PMID: 29550078 Review.
On the other hand, because of their known pathophysiological mechanisms, some well-known diseases associated with aggressive forms of CRSwNP, such as eosinophilic granulomatosis with polyangiitis, primary ciliary dyskinesia and cystic fibrosis, should be inve …
On the other hand, because of their known pathophysiological mechanisms, some well-known diseases associated with aggressive forms of CRSwNP …
In vitro culturing of ciliary respiratory cells--a model for studies of genetic diseases.
Bukowy Z, Ziętkiewicz E, Witt M. Bukowy Z, et al. J Appl Genet. 2011 Feb;52(1):39-51. doi: 10.1007/s13353-010-0005-1. Epub 2010 Dec 2. J Appl Genet. 2011. PMID: 21125367 Free PMC article. Review.
Primary ciliary dyskinesia (PCD) is a rare genetic disorder caused by the impaired functioning of ciliated cells. ...The culturing of differentiated cells and tissues derived from the human RE seems to be the best way to diagnose PCD, to study genotype-phenot
Primary ciliary dyskinesia (PCD) is a rare genetic disorder caused by the impaired functioning of ciliated cells. ...Th
Bacteriology and treatment of infections in the upper and lower airways in patients with primary ciliary dyskinesia: adressing the paranasal sinuses.
Alanin MC. Alanin MC. Dan Med J. 2017 May;64(5):B5361. Dan Med J. 2017. PMID: 28552099 Free article. Review.
The respiratory tract is lined with motile cilia that transport respiratory mucus. Primary ciliary dyskinesia (PCD) is a chronic genetic disease caused by mutations in genes responsible for ciliary structure and function. ...We revealed that P. aerugin …
The respiratory tract is lined with motile cilia that transport respiratory mucus. Primary ciliary dyskinesia (PCD) is …